MSeqDR Mitochondrial disease browser phenotype pathogenic gene and mutation portal

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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

*:HP: HPO terms, ND: NAMDC terms.
Most Studied CPEO, Complex I Deficiency, COXPD1, Leigh, LHON, MELAS, MERRF, NARP, SANDO

Disease Browser
Parent Node: benign reproductive system neoplasm (MONDO:0000383)
Parent Node: male reproductive system disease (MONDO:0003150)
..Starting node ..benign male reproductive system neoplasm ()
Child Nodes:
........benign neoplasm of epididymis ()
........benign neoplasm of penis ()
........benign neoplasm of prostate ()
........benign neoplasm of scrotum ()
........benign neoplasm of testis ()
........lipoma of spermatic cord ()
Sister Nodes:
..benign male reproductive system neoplasm ()
..cryptorchidism (disease) ()
..epididymitis (disease) ()
..fournier gangrene ()
..genital herpes ()
..hematocele of tunica vaginalis testis ()
..hydrocele ()
..male genital organ stricture ()
..male genital organ vascular disease ()
..male infertility ()
..male reproductive system neoplasm ()
..non-syndromic urogenital tract malformation of male ()
..penile disease ()
..prostate disease ()
..scrotal disease ()
..spermatocele ()
..teratozoospermia ()
..testicular disease ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	625
Name:	benign male reproductive system neoplasm
Definition:	A non-metastasizing neoplasm that arises from the male reproductive system. Representative examples include benign prostate phyllodes tumor, benign Sertoli cell tumor, seminal vesicle cystadenoma, and epididymal adenomatoid tumor.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	benign Male reproductive system neoplasm; benign Male reproductive system tumor; male reproductive organ benign neoplasm
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes: RPS24;
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal